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White Skin.” Answer the questions to help you write your summary
White Skin.” Answer the questions to help you write your summary

Heartwood extractives – from phenotype to candidate genes
Heartwood extractives – from phenotype to candidate genes

... According to earlier studies, the pinosylvin synthase gene is present in five copies in the Scots pine genome (PST-1 through PST-5; Preisig-Müller et al. 1999). All gene family members have two exons and a single intron in a conserved site. PST-1 was identified as the most active gene, which accordi ...
Slide 1
Slide 1

... Introduction: The plant as a parasite Just as some microbes and animals make their living parasitizing other organisms, many species of plants make their living by parasitizing other plants. The parasitic habit has arisen several times among flowering plant lineages. One feature that all parasitic p ...
PowerPoint Presentation - Презентация PowerPoint
PowerPoint Presentation - Презентация PowerPoint

... Biotin (vitamin H) is an essential cofactor for a class of important metabolic enzymes, biotin carboxylases and decarboxylases (Perkins and Pero 2001). Biotin biosynthetic pathway is widespread among microorganisms. The well-studied systems of biotin biosynthesis from Escherichia coli, Bacillus subt ...
Gene Name
Gene Name

... GenePix software was used to quantify fluorescence intensity for each feature and the local background on the array. Normalisation was then conducted using Gepas software (www.gepas.org) with global loess approach (Smyth and Speed, Methods 31, 265-271, 2003), which is based on the assumption that th ...
Risk Assessment for rDNA-GMMO-transgenics
Risk Assessment for rDNA-GMMO-transgenics

... has been altered in a way that does not occur naturally by mating and/or natural recombination. Genetically modified microorganism (GMMOs) refers more specifically to GMOs that are microorganisms. Transgenic animals and plants are animals or plants in which there has been a deliberate modification o ...
Patterns of Inheritance
Patterns of Inheritance

... different tissues or organs. Autosomal dominant traits are commonly pleiotropic. The diagnosis of Marfan syndrome is made based a triad of cardiovascular (aortic aneurysm, aortic insufficiency), skeletal (long limbs, fingers and toes, loose-jointedness), and eye (dislocated lens) findings. Although ...
Slide 1
Slide 1

... genes clade: #2 (ortholog_id = 17117 in panda) 159 mus genes 47 genes new to assembly 36 10 genes completely new to assembly 36 Interpro matches for this clade: !!! Expansion mainly on chr5 and 14, although single (pseudogene?) versions on chr13 and chr16. !!! Mouse DLG5 is: chr14:22,966,420-22,978, ...
Sex determination
Sex determination

... 18. Solve problems illustrating incomplete dominance, codominance (MN blood group), and multiple alleles, (human ABO blood group system) 19. Examine the effect of recessive lethal alleles on expected phenotypic ratios 20. Examine gene interactions, epistasis, effects on 9:3:3:1 ratio of dihybrid cro ...
Statistics and bioinformatics applied to omics
Statistics and bioinformatics applied to omics

... • Series of papers describing a method for analyzing the expression of sets of genes • Software available, along with a database of biologically relevant gene sets • Relatively hot topic in bioinformatics/statistics: many differerent papers and methods published on the topic, with small or large dif ...
Lec-Functional Annotation and Functional Enrichment2010
Lec-Functional Annotation and Functional Enrichment2010

... that a process must have more than one distinct steps. • A biological process is not equivalent to a pathway; at present, GO does not try to represent the dynamics or dependencies that would be required to fully describe a pathway. ...
Chapter 10: Mendel`s Laws of Heredity
Chapter 10: Mendel`s Laws of Heredity

...  Example: You have brown hair (Bb) and freckles (Ff) o You can pass on to your children one of the following combinations: B + F, b + F, ...
File
File

... Multiple-Choice Questions 1. Endocrine and paracrine signaling share which of the following properties? A) Secretion into the bloodstream B) Action upon neighboring cells * C) Activation of receptors on the cell surface or within target cells D) Secretion from endocrine glands E) Action upon cancer ...
Literome: PubMed-scale genomic knowledge base in the cloud
Literome: PubMed-scale genomic knowledge base in the cloud

... Motivation: Advances in sequencing technology have led to an exponential growth of genomics data, yet it remains a formidable challenge to interpret such data for identifying disease genes and drug targets. There has been increasing interest in adopting a systems approach that incorporates prior kno ...
File - Pearson`s Place
File - Pearson`s Place

... • Her daughters will only have the disease if they receive mom’s X chromosome that has the disease gene Y on it AND X they receive an X chromosome from dad with the disease gene on it. • They might be a carrier. • They might not be a carrier • Will her sons have the disease? ...
Introduction to DNA Microarrays
Introduction to DNA Microarrays

... – When a cell is making a protein, it translates the genes (made of DNA) which code for the protein into RNA used in its production – The RNA present in a cell can be extracted – If a gene has been expressed in a cell ...
Sem 1 Revision Chem and Biol File
Sem 1 Revision Chem and Biol File

... Gene: a chain of nucleotides that code for a protein. Chromosome: double helix containing DNA. Carries genetic information. Nucleotide: the building block of a chromosome (consists of a sugar, phosphate and a base) . Intermediate inheritance: when two characteristics are inherited to give rise to a ...
17 - Rutgers Chemistry
17 - Rutgers Chemistry

... The chloramphenicol acetyltransferase (CAT) gene is a popular reporter gene. This is a bacterial gene that evolved to protect bacteria against the antibiotic chloramphenicol (CAM). The gene encodes for a protein, chloramphenicol acetyltransferase (CAT), that can add an acetyl group (from acetyl CoA) ...
r - LT AP BIO
r - LT AP BIO

... Genotypic Ratio : 2:2 Phenotypic Ratio : 2:2 EE – 0 Free – 2 (50%) Ee – 2 (50%) Attached – 2 (50%) Ee – 2 (50%) ...
Genetic Inheritance Type Review
Genetic Inheritance Type Review

... chromosomes and can come in multiple varieties. Each variety of gene we call an allele. For example a chromosome can have an allele for brown eyes or an allele for blue eyes. In simple genetics, one allele is dominant to the others. The dominant allele (shown as a capital letter) is expressed as lon ...
What is Francisella? - Oregon State University
What is Francisella? - Oregon State University

... Reported to be part of several countries biological warfare arsenal, including the United States • Aerosolization ...
posterexample1
posterexample1

... mechanically, the fatty acid linolenic acid (18:3) is metabolized to produce the plant hormone, jasmonic acid (JA), which accumulates to high levels in wounded tissues. The JA pathway is initiated in the chloroplasts and completed in the peroxisomes. JA is then exported to the cytoplasm where it is ...
Where Do New Genes Come From? A Computational Analysis of
Where Do New Genes Come From? A Computational Analysis of

... Predict operons Identify horizontal transfers Infer functional associations Snel, Bork, Huynen. PNAS 2002 ...
Leukaemia Section t(X;11)(q22;q23)  Atlas of Genetics and Cytogenetics
Leukaemia Section t(X;11)(q22;q23) Atlas of Genetics and Cytogenetics

... Sole abnormality in AML-M2 case, part of a hyperploid karyotype associated with +6, +8, +19, +21, +21 in a child with acute megakaryoblastic leukemia and complex karyotype in ALL case associated with t(11;14)(q13;q32), and monosomy 22, indicating that the t(X;11)(q22;q23) is likely to be a secondary ...
Evolution Acts on the Phenotype
Evolution Acts on the Phenotype

... of the a allele, meaning that the a allele could be passed down to offspring. People who are carriers do not express the recessive phenotype, as they have a dominant allele. This allele is said to be kept in the population’s gene pool. The gene pool is the complete set of genes and alleles within a ...
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Gene nomenclature

Gene nomenclature is the scientific naming of genes, the units of heredity in living organisms. An international committee published recommendations for genetic symbols and nomenclature in 1957. The need to develop formal guidelines for human gene names and symbols was recognized in the 1960s and full guidelines were issued in 1979 (Edinburgh Human Genome Meeting). Several other species-specific research communities (e.g., Drosophila, mouse) have adopted nomenclature standards, as well, and have published them on the relevant model organism websites and in scientific journals, including the Trends in Genetics Genetic Nomenclature Guide. Scientists familiar with a particular gene family may work together to revise the nomenclature for the entire set of genes when new information becomes available. For many genes and their corresponding proteins, an assortment of alternate names is in use across the scientific literature and public biological databases, posing a challenge to effective organization and exchange of biological information. Standardization of nomenclature thus tries to achieve the benefits of vocabulary control and bibliographic control, although adherence is voluntary. The advent of the information age has brought gene ontology, which in some ways is a next step of gene nomenclature, because it aims to unify the representation of gene and gene product attributes across all species.Gene nomenclature and protein nomenclature are not separate endeavors; they are aspects of the same whole. Any name or symbol used for a protein can potentially also be used for the gene that encodes it, and vice versa. But owing to the nature of how science has developed (with knowledge being uncovered bit by bit over decades), proteins and their corresponding genes have not always been discovered simultaneously (and not always physiologically understood when discovered), which is the largest reason why protein and gene names do not always match, or why scientists tend to favor one symbol or name for the protein and another for the gene. Another reason is that many of the mechanisms of life are the same or very similar across species, genera, orders, and phyla, so that a given protein may be produced in many kinds of organisms; and thus scientists naturally often use the same symbol and name for a given protein in one species (for example, mice) as in another species (for example, humans). Regarding the first duality (same symbol and name for gene or protein), the context usually makes the sense clear to scientific readers, and the nomenclatural systems also provide for some specificity by using italic for a symbol when the gene is meant and plain (roman) for when the protein is meant. Regarding the second duality (a given protein is endogenous in many kinds of organisms), the nomenclatural systems also provide for at least human-versus-nonhuman specificity by using different capitalization, although scientists often ignore this distinction, given that it is often biologically irrelevant.Also owing to the nature of how scientific knowledge has unfolded, proteins and their corresponding genes often have several names and symbols that are synonymous. Some of the earlier ones may be deprecated in favor of newer ones, although such deprecation is voluntary. Some older names and symbols live on simply because they have been widely used in the scientific literature (including before the newer ones were coined) and are well established among users.
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